کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
5279231 | 1385621 | 2009 | 5 صفحه PDF | دانلود رایگان |
![عکس صفحه اول مقاله: Selective recognition of Zn2+ by salicylaldimine appended triazole-linked di-derivatives of calix[4]arene by enhanced fluorescence emission in aqueous-organic solutions: role of terminal -CH2OH moietieefs in conjunction with the imine in recognition Selective recognition of Zn2+ by salicylaldimine appended triazole-linked di-derivatives of calix[4]arene by enhanced fluorescence emission in aqueous-organic solutions: role of terminal -CH2OH moietieefs in conjunction with the imine in recognition](/preview/png/5279231.png)
A series of lower rim 1,3-di-derivatives possessing Schiff's base cores were synthesized using triazole unit as linker moiety by further introducing butyl (L2), one -CH2OH (L3) and two -CH2OH (L4)-containing moieties, respectively, in order to bring additional support for ion binding. Based on fluorescence and absorption spectroscopies it has been shown that Zn2+ could be selectively recognized by the Schiff's base core and not by the triazole core among the ten metal ions studied both in methanol and in aqueous solutions of methanol and acetonitrile, wherein the -CH2OH moieties augment the fluorescence response by providing additional coordinations to the Zn2+. Thus L4 exhibited a fluorescence enhancement of â¼65, â¼48 and â¼25-fold in methanol, aqueous solutions of methanol and acetonitrile, with minimum detection limits of 174, 313 and 320Â ppb, respectively. Both the excitation and emission wavelengths fall in visible region.
A series of lower rim 1,3-di-derivatives possessing Schiff's base cores were synthesized using triazole unit as linker moiety by further introducing butyl (L2), one -CH2OH (L3) and two -CH2OH (L4)-containing moieties respectively, in order to bring additional support for ion binding. Based on fluorescence and absorption spectroscopies it has been shown that Zn2+ could be selectively recognized by the Schiff's base core and not by the triazole core among the ten metal ions studied both in methanol and in aqueous solutions of methanol and acetonitrile, wherein the -CH2OH moieties augment the fluorescence response by providing additional coordinations to the Zn2+. Thus L4 exhibited a fluorescence enhancement of â¼65, â¼48 and â¼25-fold in methanol, aqueous solutions of methanol and acetonitrile, with minimum detection limits of 174, 313 and 320Â ppb, respectively. Both the excitation and emission wavelengths fall in visible region.
Journal: Tetrahedron Letters - Volume 50, Issue 23, 10 June 2009, Pages 2730-2734